Medical device licence · 74103 · Class 2
AUTOSCREEN IGG ASSAYS
No longer licensed: cancelled: renewal not answered
Licence status Cancelled: renewal not answered; first licensed May 18, 2007; ended December 9, 2025. It is in Health Canada’s archive of licences no longer in force.
- Licence number
- 74103
- Licence holder
- Zeus Scientific, LlcBranchburg, NJ, United States
- Risk class
- Class II (low to moderate risk)
- Licence type
- Test Kit
- First licensed
- May 18, 2007
- Ended
- December 9, 2025
- Devices covered
- 10
Devices on this licence
By name, as listed. The official record lists model numbers and identifiers.
- IFA AUTOSCREEN I (MSK/MSS) AUTOMATED IGG (AUTO. FORMAT) ASSAY (LIQUID 96)
- IFA AUTOSCREEN I (MSK/MSS) IGG ASSAY (LIQUID 48)
- IFA AUTOSCREEN I (MSK/MSS) IGG ASSAY (LIQUID 96)
- IFA AUTOSCREEN I (RK/RS) IGG ASSAY (LIQUID 48)
- IFA AUTOSCREEN I (RK/RS) IGG ASSAY (LIQUID 96)
- IFA AUTOSCREEN II (MS) IGG ASSAY (LIQUID 48)
- IFA AUTOSCREEN II (MS) IGG ASSAY (LIQUID 96)
- IFA AUTOSCREEN II (RL/RK/RS) IGG ASSAY (LIQUID 48)
- IFA AUTOSCREEN II (RL/RK/RS) IGG ASSAY (LIQUID 96)
- POSITIVE CONTROL PCA IFA ABS
Class I devices, the lowest-risk group, mostly need no device licence, so most are not in this list.